Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Coping When I Accidently Get Gluten


stephkb

Recommended Posts

stephkb Rookie

I was diagnosed with celiac in October and was doing well with the gluten free diet until I went to celebrate Thanksgiving with family, we had to drive for two days, eat on the road, eat a week and a half of meals away from home, and I am not sure how many times I got gluten while on traveling but it was at least once or twice. I then came home and accidentally got gluten from one of my pans I should have tossed but missed when I cleaned out my pantry. I seem to be very sensitive to gluten now, I think I've reacted to food with cross contamination a couple of times and am getting frustrated, as I feel that I am trying really hard to keep gluten out of my diet yet I keep getting it from somewhere.

Is there anything I can do to help me feel better when I get gluten?

Also, do you have any tips for being away from home and eating gluten free, I have to travel again at Christmas and am dreading it. I already sent back some gluten free snacks and bread for myself, but am scared about eating out and eating with people who don't normally cook gluten free. Everyone has been very nice about trying to accommodate me, but I am still very nervous after my experiences at Thanksgiving.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Lynayah Enthusiast
I was diagnosed with celiac in October and was doing well with the gluten free diet until I went to celebrate Thanksgiving with family, we had to drive for two days, eat on the road, eat a week and a half of meals away from home, and I am not sure how many times I got gluten while on traveling but it was at least once or twice. I then came home and accidentally got gluten from one of my pans I should have tossed but missed when I cleaned out my pantry. I seem to be very sensitive to gluten now, I think I've reacted to food with cross contamination a couple of times and am getting frustrated, as I feel that I am trying really hard to keep gluten out of my diet yet I keep getting it from somewhere.

Is there anything I can do to help me feel better when I get gluten?

Also, do you have any tips for being away from home and eating gluten free, I have to travel again at Christmas and am dreading it. I already sent back some gluten free snacks and bread for myself, but am scared about eating out and eating with people who don't normally cook gluten free. Everyone has been very nice about trying to accommodate me, but I am still very nervous after my experiences at Thanksgiving.

When I get glutened, the only thing that seems to help is to drink more water and take a bath in Epsom salt. Still, it doesn't take it away. Only time does that, unfortunately.

As for your having a difficult time not cheating, I am going to post here something that I posted in another thread earlier:

Depravation isn't cool. It might help to try new recipes or purchase some gluten-free items that help you feel like you're part of the group . . . and have them ready for the next time you might want to cave in and eat what the family is eating.

What are your biggest weaknesses and what can you purchase / travel with / or make that will give you similar satisfaction to the foods that tempt you to cheat?

Two things that are helping me a lot right now:

1- Letting people know that they shouldn't feel bad if I bring my own food to a get-together at their house. When I explain to them that I am so sensitive that I even have to have a dedicated can opener, their eyes pop open and they begin to understand. I ask them to PLEASE not try to do anything for me, and I explain that the risk of cross contamination is just too great . . . however, if they'd like to pour me a glass of wine, fine! I let them know that what really matters is being with them. Then I bring whatever I want and enjoy the heck out of it.

2- Talking restaurants that are not certified gluten-free into letting me bring my own food. I nicely let them know that they will have a table full of people if I can bring my own food . . . if not, we'll have to go elsewhere.

So far, I have had only one restaurant say no to me.

It helps to fit the food to the restaurant. If we go out for Mexican, I bring my own Mexican.

As odd as it sounds: There is something very liberating about going with the gluten-free flow and not trying to fit in by eating like everyone else. It takes some pre-planning, but it is worth it.

Two things happen: First, you can relax knowing that you can eat what you want without having to worry about getting sick. Second, those around you will take your gluten-intolorance more seriously and respect your needs.

Right now, I'm eating mostly whole foods only . . . however, I'm going to a family pizza / holiday cookie party in a couple weeks. I'm going to forget about my diet that night and buy a good gluten-free pizza, make it at home and bring it along. And for dessert? You guessed it, gluten-free cookies. I'll still be part of the group, but while being my own best friend.

If you'd like to view the thread this came from, it is at: https://www.celiac.com/gluten-free/index.php?showtopic=64333

The person who started the thread has similar issues with cheating. You might find it interesting.

I would add that while traveling, remember that a grocery store is often as easy to stop at as a fast food restaurant.

Also, there are some chains that offer gluten-free menus. It helps to learn them. Outback Steakhouse is one of them.

Hope this helps.

stephkb Rookie

Thanks for the tips, that is a good idea about it at restaurants. And thanks for the tip on taking a bath with Epsom salt.

I haven't actually purposely cheated, I have just accidentally gotten gluten while eating out or with family who thought they had cooked gluten free but did not actually do so. Everyone is well intentioned, and I supervised as much as possible, but I was staying in their homes and they cooked for me. I'm not sure what it was that was cooked that made me sick, and after a week of being there I am not ever sure how many times I ate things with gluten in them, but it was never on purpose, and I really was trying to avoid it. I also ate at a restaurant while home with a gluten free menu, and ordered off of it, the manager assured me they knew how to do gluten free, but my waitress was new and didn't know what she was doing, I requested corn tortillas and got flour, sent them back. I think for now I am going to try to avoid eating out or bring my own food like you suggested until I figure things out better.

When I get glutened, the only thing that seems to help is to drink more water and take a bath in Epsom salt. Still, it doesn't take it away. Only time does that, unfortunately.

As for your having a difficult time not cheating, I am going to post here something that I posted in another thread earlier:

Depravation isn't cool. It might help to try new recipes or purchase some gluten-free items that help you feel like you're part of the group . . . and have them ready for the next time you might want to cave in and eat what the family is eating.

What are your biggest weaknesses and what can you purchase / travel with / or make that will give you similar satisfaction to the foods that tempt you to cheat?

Two things that are helping me a lot right now:

1- Letting people know that they shouldn't feel bad if I bring my own food to a get-together at their house. When I explain to them that I am so sensitive that I even have to have a dedicated can opener, their eyes pop open and they begin to understand. I ask them to PLEASE not try to do anything for me, and I explain that the risk of cross contamination is just too great . . . however, if they'd like to pour me a glass of wine, fine! I let them know that what really matters is being with them. Then I bring whatever I want and enjoy the heck out of it.

2- Talking restaurants that are not certified gluten-free into letting me bring my own food. I nicely let them know that they will have a table full of people if I can bring my own food . . . if not, we'll have to go elsewhere.

So far, I have had only one restaurant say no to me.

It helps to fit the food to the restaurant. If we go out for Mexican, I bring my own Mexican.

As odd as it sounds: There is something very liberating about going with the gluten-free flow and not trying to fit in by eating like everyone else. It takes some pre-planning, but it is worth it.

Two things happen: First, you can relax knowing that you can eat what you want without having to worry about getting sick. Second, those around you will take your gluten-intolorance more seriously and respect your needs.

Right now, I'm eating mostly whole foods only . . . however, I'm going to a family pizza / holiday cookie party in a couple weeks. I'm going to forget about my diet that night and buy a good gluten-free pizza, make it at home and bring it along. And for dessert? You guessed it, gluten-free cookies. I'll still be part of the group, but while being my own best friend.

If you'd like to view the thread this came from, it is at: https://www.celiac.com/gluten-free/index.php?showtopic=64333

The person who started the thread has similar issues with cheating. You might find it interesting.

Hope this helps.

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to FannyRD's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Gluten free phosphate binders for dialysis patients

    2. - Scott Adams replied to Cecile's topic in Related Issues & Disorders
      2

      Symptoms

    3. - trents replied to Cecile's topic in Related Issues & Disorders
      2

      Symptoms

    4. - FannyRD posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Gluten free phosphate binders for dialysis patients

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,180
    • Most Online (within 30 mins)
      7,748

    Eldret419
    Newest Member
    Eldret419
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • FannyRD
      Thanks for the resource! I will check it out!
    • Scott Adams
      You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      Living with celiac disease can be especially hard when you’re in a smaller town and don’t have many people around who truly understand it, so you’re definitely not alone in feeling this way. Ongoing fatigue, joint pain, and headaches are unfortunately common in people with celiac disease, even years after diagnosis, and they aren’t always caused by gluten exposure alone. Many people find that issues like low iron, low vitamin D, thyroid problems, other autoimmune conditions, or lingering inflammation can contribute to that deep exhaustion, so it’s reasonable to push your doctor for more thorough blood work beyond just vitamin B. As for eggs, it’s also not unusual for people with celiac disease to develop additional food intolerances over time; tolerating eggs as an ingredient but not on their own can point to sensitivity to the proteins when they’re concentrated. Some people do better avoiding eggs for a while, then carefully testing them again later. Most importantly, trust your body—if something consistently makes you feel awful, it’s okay to avoid it even if it’s technically “allowed.” Many of us have had to advocate hard for ourselves medically, and connecting with other people with celiac disease, even online, can make a huge difference in feeling supported and less isolated.
    • trents
      Welcome to the celiac.com community, @Cecile! It is common for those with celiac disease to develop sensitivity/intolerance to non-gluten containing foods. There is a high incidence of this with particularly with regard to dairy products and oats but soy, eggs and corn are also fairy common offenders. Like you eggs give me problems depending on how they are cooked. I don't do well with them when fried or scrambled but they don't give me an issue when included in baked and cooked food dishes or when poached. I have done some research on this strange phenomenon and it seems that when eggs are cooked with water, there is a hydrolysis process that occurs which alters the egg protein such that it does not trigger the sensitivity/intolerance reaction. Same thing happens when eggs are included in baked goods or other cooked dishes since those recipes provide moisture.  So, let me encourage you to try poaching your eggs when you have them for breakfast. You can buy inexpensive egg poacher devices that make this easy in the microwave. For instance:  https://www.amazon.com/Poacher-Microwave-Nonstick-Specialty-Cookware/dp/B0D72VLFJR/ Crack the eggs into the cups of the poacher and then "spritz" some water on top of them after getting your fingers wet under the faucet. About 1/4 teaspoon on each side seems to work. Sprinkle some salt and pepper on top and then snap the poacher shut. I find that with a 1000 watt microwave, cooking for about 2 minutes or slightly more is about right. I give them about 130 seconds. Fatigue and joint pain are well-established health problems related to celiac disease.  Are you diligent to eat gluten-free? Have you been checked recently for vitamin and mineral deficiencies? Especially iron stores, B12 and D3. Have you had your thyroid enzyme levels checked? Are you taking any vitamin and mineral supplements? If not, you probably should be. Celiac disease is also a nutrient deficiency disease because it reduces the efficiency of nutrient absorption by the small bowel. We routinely recommend celiacs to supplement with a high potency B-complex vitamin, D3, Magnesium glycinate (the "glycinate" is important) and Zinc. Make sure all supplements are gluten-free. Finally, don't rule out other medical problems that may or may be associated with your celiac disease. We celiacs often focus on our celaic disease and assume it is the reason for all other ailments and it may not be. What about chronic fatigue syndrome for instance?
    • FannyRD
      I work as a renal RD and have a Celiac pt which has been rare for me (I might have had 3-4 Celiac pts in 15 years). I wondered if anyone can confirm that these medications are gluten free and safe for Celiac.  Ferric citrate (Auryxia)  Sucroferric oxyhydroxide (Velphoro)  lanthanum carbonate (Fosrenol) sevelamer carbonate (Renvela)   Thank you!
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.